{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Cypress",
      "address_1": "11331 Valley View St",
      "reason_for_recall": "Focus Diagnostics is recalling the Stratify JCV Dx Select due to the use of a non-conforming batch in the manufacture of JCV DxSelect EL1950 kit lot #27333. This could lead to a potential for false positive JCV results.",
      "address_2": "",
      "product_quantity": "300 units",
      "code_info": "Lot No. 27333",
      "center_classification_date": "20150417",
      "distribution_pattern": "Internationally: Denmark only.",
      "state": "CA",
      "product_description": "STRATIFY JCV DxSelect, Model No. EL1950.  Assay for detection of antibodies to JC Virus in human serum or plasma.  In Vitro diagnostic.",
      "report_date": "20150429",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Focus Diagnostics Inc",
      "recall_number": "Z-1454-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "70856",
      "termination_date": "20150723",
      "more_code_info": "",
      "recall_initiation_date": "20150315",
      "postal_code": "90630-5366",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}